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Impact of Letermovir for CMV Prophylaxis in Chinese kidney transplant patients

Impact of Letermovir for CMV Prophylaxis in Chinese kidney transplant patients

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500106690
Enrollment
Unknown
Registered
2025-07-28
Start date
2025-10-15
Completion date
Unknown
Last updated
2025-11-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

kidney transplant

Interventions

Valgancilovir group:None
Letermovir group:None

Sponsors

The First Affiliated Hospital of Xi'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients received letermovir or valganciclovir prophylaxis after kidney transplantation within 10 days and a duration of at least 90 days. 2.Age >= 18 years, male or female; 3.CMV IgG test positive and CMV DNA test negative.

Exclusion criteria

Exclusion criteria: 1.Patients with CMV infection or CMV history within 30 days before enrollment; 2.Patients with allergy to letermovir/ valganciclovir or related dosage form components; 3.Patients with severe liver damage, Child-Pugh score C; 4.Pregnant or lactating women; 5.Patients who use anti-CMV drugs within 7 days before enrollment; 6.Do not sign the informed consent; 7.Any other factors that may interfere with the study results.

Design outcomes

Primary

MeasureTime frame
Incidence of clinically significant CMV infection;

Secondary

MeasureTime frame
Incidence of CMV disease (CMV syndrome and/or tissue-invasive CMV;Time to onset of adjudicated CMV disease;Incidence of acute graft rejection, graft loss and other infections.;

Countries

China

Contacts

Public ContactDing Xiaoming

The First Affiliated Hospital of Xi'an Jiaotong University

xmding1970@163.com+86 29 85323955

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026